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SFRP1 c.*2534A>G
Variant ID: 8-41120152-T-C
NM_003012.4(
SFRP1
):c.*2534A>G
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases.
Frontiers In Cardiovascular Medicine
Ren, Huan H; Luo, Jian-Quan JQ; Ouyang, Fan F; Cheng, Li L; Chen, Xiao-Ping XP; Zhou, Hong-Hao HH; Huang, Wei-Hua WH; Zhang, Wei W
Publication Date: 2021
Variant appearance in text: rs12914
PubMed Link:
34322525
Variant Present in the following documents:
Main text
fcvm-08-675222.pdf
View BVdb publication page
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: rs12914
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page
Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.
The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12
Variant appearance in text: rs12914
PubMed Link:
24980784
Variant Present in the following documents:
Main text
View BVdb publication page